Canonical Allele Identifier: CA369856472
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950324T>C , CM000669.2:g.150950324T>C GRCh38
NC_000007.13:g.150647412T>C , CM000669.1:g.150647412T>C GRCh37
NC_000007.12:g.150278345T>C NCBI36
NG_008916.1:g.32603A>G , LRG_288:g.32603A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.1540A>G
ENST00000684241.1:n.3075A>G
ENST00000262186.10:c.2242A>G MANE Select ENSP00000262186.5:p.Lys748Glu
ENST00000330883.9:c.1222A>G ENSP00000328531.4:p.Lys408Glu
ENST00000262186.9:c.2242A>G ENSP00000262186.5:p.Lys748Glu
ENST00000330883.8:c.1222A>G ENSP00000328531.4:p.Lys408Glu
ENST00000430723.4:c.1894A>G ENSP00000387657.4:p.Lys632Glu
ENST00000461280.1:n.1529A>G
ENST00000473610.5:n.1874A>G
ENST00000532957.5:n.2465A>G
NM_000238.3:c.2242A>G , LRG_288t1:c.2242A>G NP_000229.1:p.Lys748Glu
NM_001204798.1:c.1222A>G NP_001191727.1:p.Lys408Glu
NM_172056.2:c.2242A>G , LRG_288t2:c.2242A>G NP_742053.1:p.Lys748Glu
NM_172057.2:c.1222A>G , LRG_288t3:c.1222A>G NP_742054.1:p.Lys408Glu
XM_011516185.1:c.1942A>G XP_011514487.1:p.Lys648Glu
XM_011516186.1:c.2242A>G XP_011514488.1:p.Lys748Glu
XM_011516185.2:c.1942A>G XP_011514487.1:p.Lys648Glu
XM_011516186.3:c.2242A>G XP_011514488.1:p.Lys748Glu
XM_017012195.1:c.2092A>G XP_016867684.1:p.Lys698Glu
XM_017012196.1:c.2065A>G XP_016867685.1:p.Lys689Glu
NM_000238.4:c.2242A>G MANE Select NP_000229.1:p.Lys748Glu
NM_001204798.2:c.1222A>G NP_001191727.1:p.Lys408Glu
NM_172057.3:c.1222A>G NP_742054.1:p.Lys408Glu